VU0453595
CAS No. 1432436-13-9
VU0453595( VU-0453595 | VU 0453595 )
Catalog No. M27939 CAS No. 1432436-13-9
VU0453595 is a M1 positive allosteric modulator (PAM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 57 | Get Quote |
|
| 5MG | 87 | Get Quote |
|
| 10MG | 147 | Get Quote |
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| 25MG | 286 | Get Quote |
|
| 50MG | 444 | Get Quote |
|
| 100MG | 647 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameVU0453595
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NoteResearch use only, not for human use.
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Brief DescriptionVU0453595 is a M1 positive allosteric modulator (PAM).
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DescriptionVU0453595 is a M1 positive allosteric modulator (PAM).
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In VitroApplication of M1 PAM VU0453595 (3 μM) induces a transient increase in excitability of medium spiny neurons (MSNs).
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In VivoVU0453595 potentiates M1-mediated muscarinic long-term depression (mLTD).VU0453595 (1-10?mg/kg; i.p.) reverses behavioral deficits induced by repeated phencyclidine (PCP) administration. Animal Model:Male C57BL6/J mice (8-9 weeks old)Dosage:1, 3, or 10?mg/kg Administration:Intraperitoneal (i.p.); 10?mL/kg; administered 30?min before the social interaction test Result:Rescued deficits in social interaction observed in PCP-treated mice.
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SynonymsVU-0453595 | VU 0453595
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PathwayCell Cycle/DNA Damage
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TargetAChR
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number1432436-13-9
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Formula Weight322.343
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Molecular FormulaC18H15FN4O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (310.23 mM)
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SMILESCn1cc(cn1)-c1ccc(CN2Cc3ncccc3C2=O)c(F)c1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Scott DE, et al. Small-molecule inhibitors that target protein-protein interactions in the RAD51 family of recombinases. ChemMedChem. 2015 Feb;10(2):296-303.
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